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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584827Generated: November 2, 2026

Hydrochloric Acid → HCID 15870845, compound

https://huagongshe.com/reaction/1584827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium hydrideHCID 24758—
ReactantCyclopropylamineHCID 69828—
ReactantHCID 15870855HCID 15870855—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthylorthoformateHCID 53630039—
ProductHCID 15870845HCID 15870845—

Reaction Steps

In 0.71 g of ethyl orthoformate and 0.49 g of acetic anhydride was dissolved 0.66 g of ethyl 4-[2-(benzyloxycarbonyl)isoindolin-5-yl]-2,5-difluoro-3-methoxy-6-nitrobenzoylacetate, and the solution was heated under reflux for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue obtained was dissolved in 3.3 ml of ethanol and 2 ml of methylene chloride. To the solution was added 0.08 g of cyclopropylamine, and the resulting mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue obtained was dissolved in 10 ml of tetrahydrofuran. To the solution was added 0.05 g of 60% sodium hydride, and the resulting mixture was stirred at room temperature for 30 minutes. To the reaction mixture was added 10 ml of 1N hydrochloric acid, and the crystals precipitated were collected by filtration, to obtain 0.33 g of colorless, crystalline ethyl 7-[2-(benzyloxycarbonyl)isoindolin-5-yl]-1-cyclopropyl-6-fluoro-8-methoxy-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935952
Source datasetuspto-grants-1999_08
ORD IDord-9278687abb024d8d8abcc4c9e80b60a4
Source noteuspto-grants-1999_08